| NDC Code | 0008-0833-22 |
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| Package Description | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0008-0833-22) |
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| Product NDC | 0008-0833 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Effexor |
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| Proprietary Name Suffix | Xr |
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| Non-Proprietary Name | Venlafaxine Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 19971101 |
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| End Marketing Date | 20251031 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020699 |
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| Manufacturer | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. |
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| Substance Name | VENLAFAXINE HYDROCHLORIDE |
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| Strength | 75 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
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